Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13 2
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1002922 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 1
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs10063949
SLC23A1
0.882 0.080 5 139383837 intron variant T/C snv 0.48 4
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 2
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs10117785
TNFSF15
1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34 1
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs10181042
PUS10
1.000 0.040 2 60997124 intron variant C/T snv 0.41 1
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs1020856343
SLC22A5
0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 5
rs10210302
ATG16L1
1.000 0.040 2 233250193 intron variant C/A;T snv 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10249788
LOC101927609 ; AHR
0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs10276381
JAZF1
1.000 0.040 7 28150502 intron variant C/A;T snv 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 2